Subsequent Bevacizumab Treatment in Patients With HHT. Follow up BABH

NCT ID: NCT06039124

Last Updated: 2023-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

23 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-09-01

Study Completion Date

2022-08-01

Brief Summary

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Bevacizumab is widely prescribed for the treatment of severe bleeding related to epistaxis or gastrointestinal bleeding in HHT.

We studied the efficacy of bevacizumab on severe bleeding in HHT patients in a randomized study recently published (NCT03227263, J Int Med 2023). In this study, 24 patients were included, 12 patients received bevacizumab and 12 patients received placebo. The duration of patient participation was 6 months, including the 2.5-month treatment period and 3.5 month follow-up after treatment.

We describe the evolution of the number of RBC transfused in HHT patients who received bevacizumab during the year after the end of the study.

Detailed Description

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Conditions

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Hemorrhagic Hereditary Telangiectasia HHT

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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HHT patients previously included in BABH study

Clinical and therapeutic follow-up of HHT patients for one year after the end of a clinical trial using bevacizumab.

bevacizumab treatment

Intervention Type OTHER

Descriptive study of HHT patients (bevacizumab treatment, number of RBC transfused)

Interventions

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bevacizumab treatment

Descriptive study of HHT patients (bevacizumab treatment, number of RBC transfused)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient included in BABH study

Exclusion Criteria

* Patients opposition
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sophie DUPUIS-GIROD, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospices Civils de Lyon

Locations

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Service de Médecine Interne et Maladies Vasculaires + Service Neuropédiatrie et neurochirurgie de l'enfant - CHU Angers

Angers, , France

Site Status

Hôpital Ambroise Paré

Boulogne-Billancourt, , France

Site Status

CHU de Montpellier-Hôpital St Eloi

Montpellier, , France

Site Status

Countries

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France

References

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Dupuis-Girod S, Decullier E, Riviere S, Lavigne C, Grobost V, Leguy-Seguin V, Maillard H, Chinet T, Fargeton AE, Guilhem A, Hermann R. BEST study: one-year descriptive follow-up of bevacizumab treatment in hereditary haemorrhagic telangiectasia post-BABH interventional study. Ther Adv Hematol. 2025 Apr 14;16:20406207241300828. doi: 10.1177/20406207241300828. eCollection 2025.

Reference Type DERIVED
PMID: 40290758 (View on PubMed)

Other Identifiers

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69HCL21_1438

Identifier Type: -

Identifier Source: org_study_id

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